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Showing results (851-860 of 902) with videos related to

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Structural Dynamics (Melville, N.Y.)|February 13, 2018
Photodissociation of aligned CH<sub>3</sub>I and C<sub>6</sub>H<sub>3</sub>F<sub>2</sub>I molecules probed with time-resolved Coulomb explosion imaging by site-selective extreme ultraviolet ionizationKasra Amini, Evgeny Savelyev, Felix Brauße, et al.
Human Molecular Genetics|January 31, 2015
Mosaic structural variation in children with developmental disordersDaniel A King, Wendy D Jones, Yanick J Crow, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 19, 2014
Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesityNina De Rocker, Sarah Vergult, David Koolen, et al.
Human Genetics|December 12, 2013
X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndromeR S Møller, L R Jensen, S M Maas, et al.
Brain : a Journal of Neurology|February 7, 2025
De novo and inherited variants in DDX39B cause a novel neurodevelopmental syndromeKevin T A Booth, Sharayu V Jangam, Martin M C Chui, et al.
Human Mutation|January 12, 2016
De Novo Truncating Mutations in the Kinetochore-Microtubules Attachment Gene CHAMP1 Cause Syndromic Intellectual DisabilityBertrand Isidor, Sébastien Küry, Jill A Rosenfeld, et al.
Lancet (London, England)|October 29, 2015
Neurodevelopmental outcome at 2 years of age after general anaesthesia and awake-regional anaesthesia in infancy (GAS): an international multicentre, randomised controlled trialAndrew J Davidson, Nicola Disma, Jurgen C de Graaff, et al.
Cell Death and Differentiation|July 23, 2016
ASPP2 deficiency causes features of 1q41q42 microdeletion syndromeJ Zak, V Vives, D Szumska, et al.
Plant Phenomics (Washington, D.C.)|December 19, 2025
The Global Wheat Full Semantic Organ Segmentation (GWFSS) datasetZijian Wang, Radek Zenkl, Latifa Greche, et al.
Epilepsia|September 30, 2024
POLR3B is associated with a developmental and epileptic encephalopathy with myoclonic-atonic seizures and ataxiaJoseph D Symonds, Kristen L Park, Cyril Mignot, et al.
Pageof 91

Showing results (851-860 of 902) with videos related to

Sort By:
Pageof 91
Structural Dynamics (Melville, N.Y.)|February 13, 2018
Photodissociation of aligned CH<sub>3</sub>I and C<sub>6</sub>H<sub>3</sub>F<sub>2</sub>I molecules probed with time-resolved Coulomb explosion imaging by site-selective extreme ultraviolet ionizationKasra Amini, Evgeny Savelyev, Felix Brauße, et al.
Human Molecular Genetics|January 31, 2015
Mosaic structural variation in children with developmental disordersDaniel A King, Wendy D Jones, Yanick J Crow, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 19, 2014
Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesityNina De Rocker, Sarah Vergult, David Koolen, et al.
Human Genetics|December 12, 2013
X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndromeR S Møller, L R Jensen, S M Maas, et al.
Brain : a Journal of Neurology|February 7, 2025
De novo and inherited variants in DDX39B cause a novel neurodevelopmental syndromeKevin T A Booth, Sharayu V Jangam, Martin M C Chui, et al.
Human Mutation|January 12, 2016
De Novo Truncating Mutations in the Kinetochore-Microtubules Attachment Gene CHAMP1 Cause Syndromic Intellectual DisabilityBertrand Isidor, Sébastien Küry, Jill A Rosenfeld, et al.
Lancet (London, England)|October 29, 2015
Neurodevelopmental outcome at 2 years of age after general anaesthesia and awake-regional anaesthesia in infancy (GAS): an international multicentre, randomised controlled trialAndrew J Davidson, Nicola Disma, Jurgen C de Graaff, et al.
Cell Death and Differentiation|July 23, 2016
ASPP2 deficiency causes features of 1q41q42 microdeletion syndromeJ Zak, V Vives, D Szumska, et al.
Plant Phenomics (Washington, D.C.)|December 19, 2025
The Global Wheat Full Semantic Organ Segmentation (GWFSS) datasetZijian Wang, Radek Zenkl, Latifa Greche, et al.
Epilepsia|September 30, 2024
POLR3B is associated with a developmental and epileptic encephalopathy with myoclonic-atonic seizures and ataxiaJoseph D Symonds, Kristen L Park, Cyril Mignot, et al.
Pageof 91